Autologous anti-BCMA CAR-T · relapsed/refractory multiple myeloma Phase I clinical trial

According to official protocol filings (target population synthesized by CMDN from study details, not an official CDE field), this study is primarily designed for patients with [Relapsed/refractory]. Eligibility requires verified clinical confirmation by investigators regarding prior lines of therapy, active disease biomarkers, and performance status.

According to verified protocol filings, key eligibility thresholds include: age ≥ 18 years, ECOG performance status ≤ 2, ≥ 3 prior lines of therapy. The study specifies 11 inclusion and 16 exclusion criteria covering detailed organ function and medical history. Final enrollment confirmation is determined by investigators at participating hospital trial centers.

The core therapeutic target or investigational mechanism is [Autologous anti-BCMA CAR-T]. It aims to selectively eradicate clonal plasma cells or redirect anti-tumor immune responses, representing an active area of precision hematology research.

This study is registered as a [Phase I] clinical trial. The protocol is conducted under rigorous ethical and Good Clinical Practice (GCP) oversight approved by institutional ethics committees.

This is an international multi-centre study with 0 study centres in China and 3 overseas centres. The lead institution is [Union Hospital, Tongji Medical College, Huazhong University of Science and Technology]. Prominent sites include Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, West China Hospital, Sichuan University, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences. Eligible domestic patients can seek screening at the nearest participating centre.

The official public registration identifier for this protocol is [CTR20210564] (CDE_CTR). Patients and researchers can verify registration details and regulatory authorizations directly on the official NMPA CDE platform.